Abstract

Bonding geometry engineering of metal–oxygen octahedra is a facile way of tailoring various functional properties of transition metal oxides. Several approaches, including epitaxial strain, thickness, and stoichiometry control, have been proposed to efficiently tune the rotation and tilt of the octahedra, but these approaches are inevitably accompanied by unnecessary structural modifications such as changes in thin‐film lattice parameters. In this study, a method to selectively engineer the octahedral bonding geometries is proposed, while maintaining other parameters that might implicitly influence the functional properties. A concept of octahedral tilt propagation engineering is developed using atomically designed SrRuO3/SrTiO3 (SRO/STO) superlattices. In particular, the propagation of RuO6 octahedral tilt within the SRO layers having identical thicknesses is systematically controlled by varying the thickness of adjacent STO layers. This leads to a substantial modification in the electromagnetic properties of the SRO layer, significantly enhancing the magnetic moment of Ru. This approach provides a method to selectively manipulate the bonding geometry of strongly correlated oxides, thereby enabling a better understanding and greater controllability of their functional properties.

Highlights

  • Bonding geometry engineering of metal–oxygen octahedra is a facile way of conventional lattice degree of freedom, such as lattice parameters, octahedral distailoring various functional properties of transition metal oxides

  • We report controllable octahedral tilt propagation by atomically designing artificial superlattices (SLs)

  • Variations in the magnetic easy axis are capable of influencing Ms, we confirmed that, the magnetic easy axis did not change across the structural phase transition, based on angle-dependent Hall measurements

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Summary

Introduction

Bonding geometry engineering of metal–oxygen octahedra is a facile way of conventional lattice degree of freedom, such as lattice parameters, octahedral distailoring various functional properties of transition metal oxides.

Results
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